PPT-Dr. M. A. SOFI SICKLE CELL ANEMIA

Author : grace3 | Published Date : 2022-02-14

Dr M Sofi MD FRCP London FRCPEdin FRCSEdin The term sickle cell disease SCD is generally used to describe all of the conditions associated with the phenomenon

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Dr. M. A. SOFI SICKLE CELL ANEMIA: Transcript


Dr M Sofi MD FRCP London FRCPEdin FRCSEdin The term sickle cell disease SCD is generally used to describe all of the conditions associated with the phenomenon of sickling whereas the term . &. Intercollegiate Athletics. Sickle Cell Trait. (Hereditary Condition) . Red blood cells (RBC’s) are normally round, circular or disc shaped.. RBC’s have hemoglobin component (helps carry oxygen) and platelets (helps in clotting). Jenny Pham. Protein Structure & Function. Spring 2015. Outline. Normal Adult Hemoglobin (. Hb. A). Function: Deoxygenated v. Oxygenated. Mutation in . Hb. A. Sickle Cell Hemoglobin (. Hb. S). Sickle Cell Anemia. was developed to create a greater awareness in . the Nashville . community of Sickle Cell Disease and to raise . funds for . patient care, . social services. , and research. . All . proceeds from the event . the Emergency Physician and Nurse. Sickle Cell Pain. Carlton Haywood Jr., . PhD, . MA. Core . Faculty, the Johns Hopkins Berman Institute of Bioethics. Assistant Professor, The Johns Hopkins School of Medicine. Gary Strokosch, MD. Jane Litvin, MS. Introduction. History of . sickle cell disease . (SCD). Present in Africa for at least . 5,000. . years. 1910-. . Discovered in US. Walter Clement Noel – dental student from Grenada studying in Chicago. . the Emergency Physician and Nurse. Epidemiology, Genetics, Pathophysiology. . Paula Tanabe. , PhD, RN, FAEN, FAAN. Associate Professor. Duke University, Schools of Nursing and Medicine. Objectives. Ali Al Khader, M.D.. Faculty of Medicine. Al-Balqa’ Applied University. Email: ali.alkhader@bau.edu.jo. Sickle Cell Anemia. The . most common familial hemolytic . anemia in . the . world. Sickle . cell . 1 Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTINUE PRODUCTS AND BENEFITS AT ANY TIME WITHOUT NOTICE. To qualify, a borrower must be a U.S. citizen or permanent resident i SimplicityRefinanceandconsolidateallstudentloans(bothfederalandprivate) intosingloanwithonemonthlypayment.No Feesapplicationfeesorigination feesprepaymentpenalties,disbmentfeesTheapplicationprocesssim How to apply: Find your rates at:If approved, select your rate and termUpload identity, income and loan information *Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTIN How to apply: Find your rates at:If approved, select your rate and termUpload identity, income and loan information *Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTIN 1Terms and Conditions Apply SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTINUEPRODUCTS AND BENEFITS AT ANY TIME WITHOUT NOTICE To qualify a borrower must be aUS citizen or permanent resident in an eligi (SCAFO). By Pastor Marcia Taylor, Founder, CEO. 2021. Our programs are specifically designed and dedicated to accommodating the needs of those who are faced with the challenges of Sickle Cell such as access to care, socio-economical support services, mental health, substance abuse, family and/or care provider educational support, and isolation. . Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell . anaemia. Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐.

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